Arahata K - Search Results

1

Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.

Matsumura K, Nonaka I, Tomé FM, Arahata K, Collin H, Leturcq F, Récan D, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: arahata k. Am J Hum Genet. 1993 Aug;53(2):409-16. Am J Hum Genet. 1993. PMID: 8328458 Free PMC article.

2

Partial deficiency of dystrophin-associated proteins in a young girl with sporadic myopathy and normal karyotype.

Matsumura K, Nonaka I, Arahata K, Campbell KP. Matsumura K, et al. Among authors: arahata k. Neurology. 1993 Jun;43(6):1267-8. doi: 10.1212/wnl.43.6.1267. Neurology. 1993. PMID: 8170583 No abstract available.

3

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM. Beggs AH, et al. Among authors: arahata k. Am J Hum Genet. 1991 Jul;49(1):54-67. Am J Hum Genet. 1991. PMID: 2063877 Free PMC article.

4

Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing.

Khurana TS, Prendergast RA, Alameddine HS, Tomé FM, Fardeau M, Arahata K, Sugita H, Kunkel LM. Khurana TS, et al. Among authors: arahata k. J Exp Med. 1995 Aug 1;182(2):467-75. doi: 10.1084/jem.182.2.467. J Exp Med. 1995. PMID: 7629506 Free PMC article.

5

Muscle histology in Becker muscular dystrophy.

Kaido M, Arahata K, Hoffman EP, Nonaka I, Sugita H. Kaido M, et al. Among authors: arahata k. Muscle Nerve. 1991 Nov;14(11):1067-73. doi: 10.1002/mus.880141105. Muscle Nerve. 1991. PMID: 1745279

6

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

Beggs AH, Neumann PE, Arahata K, Arikawa E, Nonaka I, Anderson MS, Kunkel LM. Beggs AH, et al. Among authors: arahata k. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):623-7. doi: 10.1073/pnas.89.2.623. Proc Natl Acad Sci U S A. 1992. PMID: 1731332 Free PMC article.

7

[Cardiomyopathy in Becker muscular dystrophy].

Sakata C, Yamada H, Sunohara N, Arahata K, Nonaka I. Sakata C, et al. Among authors: arahata k. Rinsho Shinkeigaku. 1990 Sep;30(9):952-5. Rinsho Shinkeigaku. 1990. PMID: 2265504 Japanese.

8

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.

Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Hayashi YK, et al. Among authors: arahata k. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

9

Immunocytochemical analysis of dystrophin in congenital muscular dystrophy.

Arikawa E, Ishihara T, Nonaka I, Sugita H, Arahata K. Arikawa E, et al. Among authors: arahata k. J Neurol Sci. 1991 Sep;105(1):79-87. doi: 10.1016/0022-510x(91)90122-n. J Neurol Sci. 1991. PMID: 1795174

10

[A case of Becker muscular dystrophy presenting cardiac failure as an initial symptom].

Sakata C, Sunohara N, Nonaka I, Arahata K, Sugita H. Sakata C, et al. Among authors: arahata k. Rinsho Shinkeigaku. 1990 Feb;30(2):210-3. Rinsho Shinkeigaku. 1990. PMID: 2190744 Review. Japanese.

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